# Bemis Health Care

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1976–1989): 12 510(k) clearances
- Product codes: BYZ (2), FOB (1), JOL (1), LDQ (1), FNY (1), FRG (1), FNP (1), GCX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K885019: Bemis Sterile-Case for Use W/Ethylene Oxide Steri. (Jan 25, 1989)
- K822557: Specimen Adaptor (Oct 18, 1982)
- K822556: Critical Measurement Unit (Oct 18, 1982)
- K803206: Suction Probe (Jan 21, 1981)
- K771737: Suction Canister (Dec 20, 1977)
- K771733: 8 Emesis Basin (Sep 28, 1977)
- K771738: Male Urinal (Sep 28, 1977)
- K760393: Bed Pan, Stackable (Autoclavable) (Aug 23, 1976)

Source page: https://510kreport.com/company/bemis-health-care